SCN8A splicing mutation causing skipping of the exon 15 associated with intellectual disability and cortical myoclonus

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)56-58
Number of pages3
JournalSeizure
Volume82
DOIs
Publication statusPublished - Nov 2020

Keywords

  • Myoclonus
  • Progressive myoclonus epilepsy
  • SCN8A gene
  • Sodium channelopathy

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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